Michael F. Wangler

8.4k citations

62 papers · 1.8k indexed · h-index 25

Molecular Biology top 10%
Genetics top 5%
Pediatrics, Perinatology and Child Health top 5%
Clinical Biochemistry top 2%
Epidemiology

Co-authors: Hugo J. Bellen Shinya Yamamoto Michael R. DeBaun Andrew P. Feinberg Aimee S. Chang Kelle H. Moley Ann B. Moser Nancy Braverman
Topics: Genomics and Rare Diseases (15 papers)Peroxisome Proliferator-Activated Receptors (15 papers)Genetics and Neurodevelopmental Disorders (10 papers)
Cited by: Aging Clinical Biochemistry Genetics
Journals: SHILAP Revista de lepidopterologíaPLoS ONE Nature Reviews Genetics
Partner nations: United States Canada China

In The Last Decade

Michael F. Wangler

60 papers receiving 1.7k citations

Peers

Countries citing papers authored by Michael F. Wangler

Since Specialization

Citations

This map shows the geographic impact of Michael F. Wangler's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Michael F. Wangler with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Michael F. Wangler more than expected).

Fields of papers citing papers by Michael F. Wangler

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Michael F. Wangler. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Michael F. Wangler. The network helps show where Michael F. Wangler may publish in the future.

Co-authorship network of co-authors of Michael F. Wangler

This figure shows the co-authorship network connecting the top 25 collaborators of Michael F. Wangler. A scholar is included among the top collaborators of Michael F. Wangler based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Michael F. Wangler. Michael F. Wangler is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	De novo variants in CDKL1 and CDKL2 are associated with neurodevelopmental symptoms 2025 ·The American Journal of Human Genetics ·(unknown),(unknown),Daniel F. Eberl,Güney Bademci,(unknown),Stephanie Bivona,(unknown),(unknown),Michael F. Wangler,Shane McKee,Mustafa Tekin,Hugo J. Bellen,Oguz Kanca	1
2	Novel hemizygous single‐nucleotide duplication in RPGR in a patient with retinal dystrophy and sensorineural hearing loss 2024 ·Molecular Genetics & Genomic Medicine ·(unknown),(unknown),Liesbeth Vossaert,Nichole Owen,Richard A. Lewis,(unknown),(unknown),Michael F. Wangler,Sandesh C.S. Nagamani	1
3	Dicarboxylic acylcarnitine biomarkers in peroxisome biogenesis disorders 2023 ·Molecular Genetics and Metabolism ·Michael F. Wangler,(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Marcus J. Miller	3
4	A de novo missense variant in EZH1 associated with developmental delay exhibits functional deficits in Drosophila melanogaster 2023 ·Genetics ·(unknown),Lauren C. Briere,(unknown),(unknown),Melissa Walker,Lance H. Rodan,Frances A. High,(unknown),Shinya Yamamoto,David A. Sweetser,Michael F. Wangler	6
5	Precision therapy for a medically actionable ATP1A3 variant from a genomic medicine program in an underserved population 2023 ·Molecular Genetics & Genomic Medicine ·(unknown),Rebecca O. Littlejohn,(unknown),(unknown),(unknown),Liesbeth Vossaert,Nichole Owen,Michael F. Wangler,(unknown),(unknown)	1
6	Clinical diagnosis of metabolic disorders using untargeted metabolomic profiling and disease-specific networks learned from profiling data 2022 ·Scientific Reports ·(unknown),Xiqi Li,Lindsay C. Burrage,Kevin Riehle,Joseph G. Hacia,Nancy Braverman,Michael F. Wangler,Marcus J. Miller,Sarah H. Elsea,Aleksandar Milosavljevic	18
7	Model organisms contribute to diagnosis and discovery in the undiagnosed diseases network: current state and a future vision 2021 ·Orphanet Journal of Rare Diseases ·(unknown),Dustin Baldridge,Michael F. Wangler,(unknown),Shinya Yamamoto,Tim Schedl,Stephen C. Pak,John H. Postlethwait,Jimann Shin,Lilianna Solnica‐Krezel,Hugo J. Bellen,Monte Westerfield	49
8	A Genetic Screen for Genes That Impact Peroxisomes in Drosophila Identifies Candidate Genes for Human Disease 2019 ·G3 Genes Genomes Genetics ·Hillary K. Graves,(unknown),Kai Li Tan,Antonella Pignata,Elaine Seto,Shinya Yamamoto,Michael F. Wangler	7
9	Xia–Gibbs syndrome in adulthood: a case report with insight into the natural history of the condition 2019 ·Molecular Case Studies ·David R. Murdock,Yunyun Jiang,Michael F. Wangler,Michael M. Khayat,Aniko Sabo,Jane Juusola,Kirsty McWalter,(unknown),Meral Gunay‐Aygun,Richard A. Gibbs	13
10	De novo missense variant in the GTPase effector domain (GED) of DNM1L leads to static encephalopathy and seizures 2019 ·Molecular Case Studies ·Nurit Assia Batzir,(unknown),Tanya N. Eble,Pengfei Liu,Christine M. Eng,Sarah H. Elsea,Laurie Robak,Fernando Scaglia,Alica M. Goldman,Shweta U. Dhar,Michael F. Wangler	26
11	An SCN1B Variant Found in a Child Diagnosed with Epilepsy and Brugada Syndrome Modifies Brain-Type (NaV1.1) and Cardiac-Type (NaV1.5) Sodium Currents 2018 ·Biophysical Journal ·(unknown),Helena Riuró,Elisabet Selga,Michael F. Wangler,Ramón Brugada,Guillermo J. Pérez,Fabiana S. Scornik	1
12	Inborn Errors of Metabolism Involving Complex Molecules 2018 ·Pediatric Clinics of North America ·Cinzia Maria Bellettato,Leroy Hubert,Maurizio Scarpa,Michael F. Wangler	17
13	A metabolomic map of Zellweger spectrum disorders reveals novel disease biomarkers 2018 ·Genetics in Medicine ·Michael F. Wangler,Leroy Hubert,Taraka Donti,(unknown),Marcus J. Miller,Nancy Braverman,(unknown),Mousumi Bose,Ann B. Moser,Richard O. Jones,William B. Rizzo,V. Reid Sutton,Qin Sun,Adam D. Kennedy,Sarah H. Elsea	43
14	Peroxisomal biogenesis is genetically and biochemically linked to carbohydrate metabolism in Drosophila and mouse 2017 ·PLoS Genetics ·Michael F. Wangler,(unknown),Vafa Bayat,Νικόλαος Γιαγτζόγλου,(unknown),Nagireddy Putluri,Cristian Coarfa,Taraka Donti,Brett H. Graham,Joseph E. Faust,James A. McNew,Ann B. Moser,Marco Sardiello,Myriam Baes,Hugo J. Bellen	32
15	Diagnosis of a mild peroxisomal phenotype with next-generation sequencing 2016 ·Molecular Genetics and Metabolism Reports ·(unknown),Dianna K. Wheaton,Mingchu Xu,David G. Birch,Sara J. Bowne,Lori S. Sullivan,Stephen P. Daiger,(unknown),Richard O. Jones,Ann B. Moser,Rui Chen,Michael F. Wangler	27
16	Diagnosis of adenylosuccinate lyase deficiency by metabolomic profiling in plasma reveals a phenotypic spectrum 2016 ·Molecular Genetics and Metabolism Reports ·Taraka Donti,Gerarda Cappuccio,Leroy Hubert,Juanita Neira,Paldeep S. Atwal,Marcus J. Miller,Aaron L. Cardon,V. Reid Sutton,Brenda E. Porter,Fiona M. Baumer,Michael F. Wangler,Qin Sun,Lisa Emrick,Sarah H. Elsea	49
17	Fruit Flies in Biomedical Research 2015 ·Genetics ·Michael F. Wangler,Shinya Yamamoto,Hugo J. Bellen	124
18	Dataset for a case report of a homozygous PEX16 F332del mutation 2015 ·Data in Brief ·Carlos A. Bacino,(unknown),Elaine Seto,Tim Lotze,Fan Xia,Richard O. Jones,Ann B. Moser,Michael F. Wangler	2
19	Fibrochondrogenesis Results from Mutations in the COL11A1 Type XI Collagen Gene 2010 ·The American Journal of Human Genetics ·Stuart W. Tompson,Carlos A. Bacino,Nicole P. Safina,Michael B. Bober,Virginia K. Proud,Tara Funari,Michael F. Wangler,Lisette Nevarez,Leena Ala‐Kokko,William R. Wilcox,David R. Eyre,Deborah Krakow,Daniel H. Cohn	54
20	Racial disparity in the frequency of recurrence of preterm birth 2007 ·American Journal of Obstetrics and Gynecology ·Zachary A.-F. Kistka,Lisanne Palomar,(unknown),Sarah Boslaugh,Michael F. Wangler,F. Sessions Cole,Michael R. DeBaun,Louis J. Muglia	152

About Michael F. Wangler

Michael F. Wangler is a scholar working on Clinical Biochemistry, Genetics and Molecular Biology, having authored 62 papers that have together received 1.8k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (15 papers), Peroxisome Proliferator-Activated Receptors (15 papers) and Genetics and Neurodevelopmental Disorders (10 papers). The work is most often cited by research in Aging (93 citations), Clinical Biochemistry (202 citations) and Genetics (526 citations). Michael F. Wangler has collaborated with scholars based in United States, Canada and China. Frequent co-authors include Hugo J. Bellen, Shinya Yamamoto, Michael R. DeBaun, Andrew P. Feinberg, Aimee S. Chang, Kelle H. Moley, Ann B. Moser, Nancy Braverman, Hsiao‐Tuan Chao and Mousumi Bose. Their work appears in journals such as SHILAP Revista de lepidopterología, PLoS ONE and Nature Reviews Genetics.

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